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Author Details

Jeanette J McCarthy
Fabric Genomics Inc.
2000
50
24
PMIDPaper TitleJournal TitlePublished Year
34645491Artificial intelligence enables comprehensive genome interpretation and nomination of candidate diagnoses for rare genetic diseases.Genome Med2021
29927353A note from the editors.Per Med2018
26810587Toward clinical genomics in everyday medicine: perspectives and recommendations.Expert Rev Mol Diagn2016
26411302Clinical application of pharmacogenetics: focusing on practical issues.Pharmacogenomics2015
25614866Driving personalized medicine forward: the who, what, when, and how of educating the health-care workforce.Mol Genet Genomic Med2014
23761042Genomic medicine: a decade of successes, challenges, and opportunities.Sci Transl Med2013
23701538Development and evaluation of a genetic risk score for obesity.Biodemography Soc Biol2013
21185108The Alzheimer's associated 5' region of the SORL1 gene cis regulates SORL1 transcripts expression.Neurobiol Aging2012
22898894Pleiotropy and allelic heterogeneity in the TOMM40-APOE genomic region related to clinical and metabolic features of hepatitis C infection.Hum Genet2012
22559859Metaprotein expression modeling for label-free quantitative proteomics.BMC Bioinformatics2012
22359560Characterization of the poly-T variant in the TOMM40 gene in diverse populations.PLoS One2012
21735316Serum apolipoprotein C-III is independently associated with chronic hepatitis C infection and advanced fibrosis.Hepatol Int2012
20642483Sex and age differences in lipid response to chronic infection with the hepatitis C virus in the United States National Health and Nutrition Examination Surveys.J Viral Hepat2011
22011848Thrombospondin-4 polymorphism (A387P) predicts cardiovascular risk in postinfarction patients with high HDL cholesterol and C-reactive protein levels.Thromb Haemost2011
21703198Beneficial IL28B genotype associated with lower frequency of hepatic steatosis in patients with chronic hepatitis C.J Hepatol2011
21750736Characterization of serum proteins associated with IL28B genotype among patients with chronic hepatitis C.PLoS One2011
21381069High predictive accuracy of an unbiased proteomic profile for sustained virologic response in chronic hepatitis C patients.Hepatology2011
21046180The effect of SNCA 3' region on the levels of SNCA-112 splicing variant.Neurogenetics2011
21253498Gene by sex interaction for measures of obesity in the framingham heart study.J Obes2011
20085651Impact of gene variants on sex-specific regulation of human Scavenger receptor class B type 1 (SR-BI) expression in liver and association with lipid levels in a population-based study.BMC Med Genet2010
20890887Hepatitis C trials that combine investigational agents with pegylated interferon should be stratified by interleukin-28B genotype.Hepatology2010
20442857Genome-wide association study of Lp-PLA(2) activity and mass in the Framingham Heart Study.PLoS Genet2010
20637200A polymorphism near IL28B is associated with spontaneous clearance of acute hepatitis C virus and jaundice.Gastroenterology2010
20176026Replicated association between an IL28B gene variant and a sustained response to pegylated interferon and ribavirin.Gastroenterology2010
20235331Interferon-lambda genotype and low serum low-density lipoprotein cholesterol levels in patients with chronic hepatitis C infection.Hepatology2010
19276229Polymorphisms of the scavenger receptor class B member 1 are associated with insulin resistance with evidence of gene by sex interaction.J Clin Endocrinol Metab2009
22461094Transforming the practice of medicine using genomics.Clin Cases Miner Bone Metab2009
19606541Racial differences in the interaction between family history and risk factors associated with diabetes in the National Health and Nutritional Examination Survey, 1999-2004.Genet Med2009
17306735Gene by sex interaction in the etiology of coronary heart disease and the preceding metabolic syndrome.Nutr Metab Cardiovasc Dis2007
18370780Family History of Diabetes, Acculturation, and the Metabolic Syndrome among Mexican Americans: Proyecto SALSA.Metab Syndr Relat Disord2007
17940228Validity of reported genetic risk factors for acute coronary syndrome.JAMA2007
17765118Taking cardiovascular genetic association studies to the next level.J Am Coll Cardiol2007
15757620Aspirin resistance and a single gene.Am J Cardiol2005
16273067Life, diversity and the pursuit of haplotypes.Nat Biotechnol2005
15910850Modification of the effects of estrogen therapy on HDL cholesterol levels by polymorphisms of the HDL-C receptor, SR-BI: the Rancho Bernardo Study.Atherosclerosis2005
16018837Atherosclerotic risk genotypes and recurrent coronary events after myocardial infarction.Am J Cardiol2005
15094117Coronary artery disease and the thrombospondin single nucleotide polymorphisms.Int J Biochem Cell Biol2004
15121769Large scale association analysis for identification of genes underlying premature coronary heart disease: cumulative perspective from analysis of 111 candidate genes.J Med Genet2004
15075536Amino acid residue at position 13 in HLA-DR beta chain plays a critical role in the development of Kaposi's sarcoma in AIDS patients.AIDS2004
15131549Replication of the association between the thrombospondin-4 A387P polymorphism and myocardial infarction.Am Heart J2004
12807968Association of genetic variants in the HDL receptor, SR-B1, with abnormal lipids in women with coronary artery disease.J Med Genet2003
14566094Polymorphisms of the HDL receptor gene associated with HDL cholesterol levels in diabetic kindred from three populations.Hum Hered2003
14557872Evidence for substantial effect modification by gender in a large-scale genetic association study of the metabolic syndrome among coronary heart disease patients.Hum Genet2003
14668540Advances in pharmacogenomic research and development.Mol Biotechnol2003
11711191Personalized medicine: revolutionizing drug discovery and patient care.Trends Biotechnol2001
11208852Melastatin expression and prognosis in cutaneous malignant melanoma.J Clin Oncol2001
11723011Single nucleotide polymorphisms in multiple novel thrombospondin genes may be associated with familial premature myocardial infarction.Circulation2001
10802616The use of single-nucleotide polymorphism maps in pharmacogenomics.Nat Biotechnol2000
11121834The true nature of pharmacogenomic associations?Trends Pharmacol Sci2000
11058782Genetic studies: look no further than your own backyard.Trends Biotechnol2000
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Collaborators

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University of Minnesota Genomics Center (UMNGC)
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Boston Children's Hospital
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University of Utah
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Co-authored papers 1
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Co-authored papers 1
Washington University School of Medicine
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Brigham and Women's Hospital, Harvard Medical School
Co-authored papers 1
University of California, Rady Children's Hospital San Diego
Co-authored papers 1
Clinical & Policy
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